Author

E.-A. Bae

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Immunology· 1

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Research Focus:cancer & tumor microenvironment· 1 Approach:experimental assay· 1 Organism:human· 1

Frequent Co-Authors

A. B. Palete· 1 shared A. R. Campos· 1 shared A. Rao· 1 shared C. J. Stairiker· 1 shared D. C. Otero· 1 shared E. S. Wang· 1 shared H. A. Faso· 1 shared H. Seo· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperImmunology

A. B. Palete

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1 paper

Recent·Most cited

PSGL-1 directs early TCR signaling to repress metabolism and promote T cell exhaustion by modulating the TCF-1/TOX axis in CD8+ T cells.

J. L. Hope, D. C. Otero, E.-A. Bae, C. J. Stairiker, A. B. Palete, H. A. Faso, M. L. Henriquez, H. Seo, X. Lei, E. S. Wang, R. Tinoco, A. R. Campos, J. Yin, P. D. Adams, A. Rao, L. M. Bradley

This study shows PSGL-1 modulates TCF-1/TOX axis to repress metabolism and promote T cell exhaustion in CD8+ T cells, making it a therapeutic target for PD-1/PD-L1 resistant tumors.

bioRxiv · Jan 24, 2022 · PreprintImmunology